Search research articles
Contact Us
Filters
Showing results (1-10 of 103) with videos related to
Page
of 11
Sort By:
Annals of Vascular Diseases
|
June 26, 2024
Hereditary Aortic Aneurysms and Dissections: Clinical Diagnosis and Genetic Testing
Hiroko Morisaki
Nihon Rinsho. Japanese Journal of Clinical Medicine
|
April 16, 2008
[Urate production and regulation]
Takayuki Morisaki, Hiroko Morisaki
Journal of Human Genetics
|
October 9, 2015
Genetics of hereditary large vessel diseases
Takayuki Morisaki, Hiroko Morisaki
Nihon Rinsho. Japanese Journal of Clinical Medicine
|
April 16, 2008
[AMPD genes and urate metabolism]
Hiroko Morisaki, Takayuki Morisaki
Journal of General and Family Medicine
|
December 22, 2017
A case of fulminant type 1 diabetes masquerading acute pancreatitis
Naoki Matsuura, Shumpei Yoshino, Hiroko Morisaki
Biochemical and Biophysical Research Communications
|
April 15, 2004
Single-nucleotide polymorphism g.1548G > A (E469K) in human ICAM-1 gene affects mRNA splicing pattern and TPA-induced apoptosis
Mutsumi Iwao, Hiroko Morisaki, Takayuki Morisaki
Internal Medicine (Tokyo, Japan)
|
February 23, 2026
Double Mutations in the FLNA and MYH11 Genes Causing Familial Thoracic Aortic Aneurysm and Dissection: A Report of Two Cases
Nobuhiro Ogasawara, Wakana Sato, Hiroko Morisaki, et al.
Cardiology in the Young
|
July 22, 2011
Prenatal complex congenital heart disease with Loeys-Dietz syndrome
Yukiko Kawazu, Noboru Inamura, Futoshi Kayatani, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
September 21, 2021
Nonsurgical treatment of cerebral ischemia associated with ACTA2 cerebral arteriopathy: a case report and literature review
Ai Muroi, Junko Shiono, Satoshi Ihara, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
January 15, 2025
A novel in-frame deletion flanking exon 54 of the FBN1 gene in a Japanese girl with Marfan syndrome
Toshihiko Mori, Shigeto Fuse, Kazuna Hirai, et al.
Page
of 11
Search research articles
Search
Showing results (1-10 of 103) with videos related to
Sort By:
Page
of 11
Annals of Vascular Diseases
|
June 26, 2024
Hereditary Aortic Aneurysms and Dissections: Clinical Diagnosis and Genetic Testing
Hiroko Morisaki
Nihon Rinsho. Japanese Journal of Clinical Medicine
|
April 16, 2008
[Urate production and regulation]
Takayuki Morisaki, Hiroko Morisaki
Journal of Human Genetics
|
October 9, 2015
Genetics of hereditary large vessel diseases
Takayuki Morisaki, Hiroko Morisaki
Nihon Rinsho. Japanese Journal of Clinical Medicine
|
April 16, 2008
[AMPD genes and urate metabolism]
Hiroko Morisaki, Takayuki Morisaki
Journal of General and Family Medicine
|
December 22, 2017
A case of fulminant type 1 diabetes masquerading acute pancreatitis
Naoki Matsuura, Shumpei Yoshino, Hiroko Morisaki
Biochemical and Biophysical Research Communications
|
April 15, 2004
Single-nucleotide polymorphism g.1548G > A (E469K) in human ICAM-1 gene affects mRNA splicing pattern and TPA-induced apoptosis
Mutsumi Iwao, Hiroko Morisaki, Takayuki Morisaki
Internal Medicine (Tokyo, Japan)
|
February 23, 2026
Double Mutations in the FLNA and MYH11 Genes Causing Familial Thoracic Aortic Aneurysm and Dissection: A Report of Two Cases
Nobuhiro Ogasawara, Wakana Sato, Hiroko Morisaki, et al.
Cardiology in the Young
|
July 22, 2011
Prenatal complex congenital heart disease with Loeys-Dietz syndrome
Yukiko Kawazu, Noboru Inamura, Futoshi Kayatani, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
September 21, 2021
Nonsurgical treatment of cerebral ischemia associated with ACTA2 cerebral arteriopathy: a case report and literature review
Ai Muroi, Junko Shiono, Satoshi Ihara, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
January 15, 2025
A novel in-frame deletion flanking exon 54 of the FBN1 gene in a Japanese girl with Marfan syndrome
Toshihiko Mori, Shigeto Fuse, Kazuna Hirai, et al.
Page
of 11